http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2009327349-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0597f9c318d2aeca86db94711c516383
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-08
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-08
filingDate 2009-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a11e14ccb02668e86544e3a97661861
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e4d917671d7aa2132c260dd8f5628edc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07aa647c8da9bed4a1d7d33d1268c475
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_718d9a3d48a90036b54e09116b02011f
publicationDate 2012-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2009327349-B2
titleOfInvention Method for the preparation of 1-acetyl-6-amino-3, 3-dimethyl-2, 3 -dihydroindole
abstract The present invention relates to processes for preparing indoline compounds, comprising the steps of:a) reacting formula (I) and formula (II) to form a hydrazone; b) cyclization of the hydrazone in the presence of a Fischer catalyst to form a 3H-indole; c) reduction of the 3H-indole to form a 2,3-dihydro-indole; d) nitration of the 2,3-dihydro-indole to form a 6-nitro-2,3-dihydro-indole; e) acylation of the 6-nitro-2,3-dihydro-indole to form the protected 6-nitro-2,3- dihydro-indole; and f) conversion of the nitro group to form 6-amino-2,3-dihydro-indole.
priorityDate 2008-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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